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Abraham
Flexner on staff at the
Carnegie
Foundation, and funded by the
Rockefeller
Foundation, 'sourced' the American 'medical' reformation following US
Congressional acceptance of the "Flexner Report."
This infamous treatise exclusively benefited the
IG Farben/Rockefeller
petrochemical pharmaceutical alliance that vilified every form of natural
healing, replacing nutrition with
petrochemicals to monopolize
healthcare.
In her 1993 book The
Molecular Vision of Life, Dr. Lily E. Kay, whom a 2001 MIT News Office
obituary referred to as "one of the outstanding historians of biology of her
generation," argued that the "new biology" was largely forged by the
Rockefeller Foundation and its subsidiary program at the California Institute
of Technology (Caltech) through a consensus between a scientific elite and a
business elite whose broader aims centered on eugenics and the need to create a
mechanism of social control and human engineering:
"The new science did
not just evolve by natural
selection of randomly distributed disciplinary variants, nor did it ascend
solely through the compelling power of its ideas and its leaders. Rather, the
rise of the new biology was an expression
of the systematic cooperative efforts of America's scientific establishment
- scientists and their patrons - to direct
the study of animate
phenomena along selected paths toward a shared vision of science and
society." - Dr. Lily E. Kay
Practioners of alternative
healing methods consider the application of chemical toxins and surgeries to be
'allopathic medicine'.
"The Allopathic approach to healing is a far cry
from Hippocratic method of healing which attempted to use natural methods of
balancing 'humors.'
"The term "allopathy" was invented by German
physician Samuel Hahnemann.
He conjoined allos "opposite" and pathos
"suffering" as a referent to harsh medical practices of his era which included
bleeding, purging, vomiting and
the administration of
highly toxic drugs.
These practices were
based on the ancient Greek humoral theory which attributed disease to an
imbalance of four humors (i.e., blood, phlegm, and black and yellow bile) and
four bodily conditions (i.e, hot, cold,
wet and dry) that corresponded
to four elements (earth,
air, fire, and water).
Physicians following the Hippocratic tradition attempted to balance the
humors by treating symptoms with "opposites." - William Jarvis
Reliance on toxic chemical drugs is based
upon the philosophy of Santorio Santorio, also known as Sanctorius.
Santorio argued throughout his career that the
fundamental properties of human health were
mathematical ones, such as number,
position, and form - breaking from describing the body and its functions in
terms of Aristotelian (and Galenic) elements and qualities.
This
radical break with traditional medical theory and natural philosophy proposed
the human body was a machine the workings of which were determined by the
shapes and positions of its interlocking parts that could be broken down into
constituent molecules.
Beginning from a
fundamentally unsound foundation Santorio made 'phenomenal' properties, seen
from a mechanistic Newtonian
viewpoint, central to his worldview of
nature and
medicine.
While the central
metaphor of Aristotelian natural philosophy and Galenic medicine was organic,
Santorio made it mechanical: the
clock (more generally,
the machine) became the
metaphor for nature opening up a window for
biochemistry and, later,
molecular biology.
While his 'trail and error' experiments were
replicated and augmented by his followers and finally surpassed by those of
Antoine Lavoisier he is still regarded by many as the father of
experimental
physiology.
"How does a physician subscribing to "first do no harm" find himself or herself
prescribing either drugs that are inherently harmful or drugs at hazardous
levels?
The answer is not complex.
" Follow the money" is all
one needs to do." - Tom Pula
"When patients ask for a drug, they tend to get the
drug regardless of whether it is appropriate for them." -
Joel Weissman, health policy expert
"According to the 2005 Partnership Attitude
Tracking Study, 40% believe that prescription medicines are
"much safer" to use than
illegal drugs.
These controlled substances are not just highly
dangerous, but they can prove lethal." -
Joseph T. Rannazzisi, May 16, 2007
1990 Americans spend $40 billion on
prescription
medications.
1998
JAMA study estimates 106,000
prescription
medication deaths.
2004 Americans spend $190
billion on prescription
medications.
2006 Americans spend $280
billion on prescribed
medications.
2009 FDA
approves distribution of medical journal articles by
pharmaceutical manufacturers
describing unapproved off-label uses of drugs.
2011
Record
4.02 billion prescriptions in US
2015
Americans spend $413 billion on prescribed drugs.
Over
1000% increase in twenty five years.
80% of the active pharmaceutical ingredients used to make drugs sold
in America are imported and 40% of
finished drugs are made in foreign countries - much of both from
China.
"Apothecary, n.
The physicians's accomplice,
undertaker's benefactor and grave worm's provider."
Ambrose
Bierce
The US Chamber of Commerce and the
Pharmaceutical Research and Manufacturers of America ("PHRMA") argue
that exposing generic pharmaceutical manufacturers to state law tort liability
will negatively impact the American healthcare system by denying physicians and
patients in some states access to certain generic medications.
Under
the Supremacy Clause of the US Constitution, federal laws represent the supreme
law of the land and may preempt
or override state laws.
1984 Hatch-Waxman
Act allows generic drug makers to bypass extensive testing requirements and
enter the market if they can prove that their generic drug is equivalent to an
approved brand-name drug and
carries the same labeling.
1992 Prescription
Drug User Fee Act (PDUFA) is marketed for its miraculous ability to reduce
the time and cost of bringing lifesaving drugs to market in time to save
substantial numbers of 'disease' victims.
June 23,
2011 PLIVA, Inc. v. Mensing
Federal drug regulations
applicable to generic drug manufacturers directly conflict with, and thus
preempt, state-law tort claims alleging a failure to provide adequate warning
labels.
Supreme
Court holds that the "sameness" requirement of the Hatch-Waxman Act preempt
state law duties that imposed stricter labeling requirements on generic drugs.
Supreme Court rules that federal law related to pharmaceutical
regulations preempts a person's ability to sue in state courts and allege that
a generic drug is poorly designed and manufactured.
Supreme Court rules
that the FDA has authority over
pharmaceuticals.
80% of all drugs consumed
in the US are now exempt
from liability for side
effects, mislabeling and virtually any
other adverse
reactions.
Generic pharmaceutical manufatures no longer have to
worry about safety or side
effects, they are exempt from the multi-million dollar court-imposed
settlements awarded to victims of their generic drugs.
"Today's court
decision provides a disincentive for generic makers of drugs to monitor safety
of their products and to make sure that they have a surveillance system in
place to detect adverse events that pose a threat to patients." - Michael
Carome, Public Citizen's Health Research Group
June 24,
2013 Mutual Pharmaceutical Co. v. Bartlett
Generic drug
manufactures cannot be held liable under state law for not adequately labeling
medication when federal law prohibits them from changing the label from the
original brand name drug.
(Choose two or more of the above to comply with
Obamacare.)
If the FDA rules a drug is safe,
even if it
kills a loved one,
(or a loved one kills you !)
you have no recourse !
"Sick days are typically unplanned, which results
in significant burdens to corporations when individuals do not show up as
expected." - Rick Chaifetz, CEO of ComPysch
"People are being forced to chose between being
a good employee or being
a good family member.
That's not
a choice anyone should have to make." - Linda Meric, director of 9 to 5,
National Association of Working Women
Commercial messages are ingrained by
endlessly repetition.
To understand how social control through
prescribed petrochemical pharmaceuticals works one must understand common human
dreams.
Human aspire
for immortality, to be elevated into a position outside of nature, where
natural physical laws are preempted and life continues
eternally.
PHRMA uses this common unnatural human desire and sells
the idea of beating death with petrochemical pharmaceuticals.
But many
commonly prescribed pharmaceuticals promote cancer !
Hormone replacement therapy is among
the most controversial medications.
Industrially produced estrogen can promote
uterine as well as
breast
cancer.
Many pharmaceuticals have warnings about
cancer creation.
Omeprazole (Prilosec©) causes
abnormal cell growth and stomach
tumors (carcinoids) in rats.
Spironolactone (Aldactazide©,
Aldactone©) a blood
pressure medicine, sometimes prescribed for hormonal imbalances and facial
hair growth in women, causes tumors in rats.
Elidel© and Protopic©, are
associated with lymmphoma and skin cancer.
The rheumatoid
arthritis injections Cimzia©, Enbrel©, Humira© and
Remicade©, expensive bio-tech drugs have been associated with
lymphoma.
"In the
New England Journal of Medicine, Sept. 25, 2008, investigators noted a
higher incidence of cancer in subjects taking
Vytorin©." - Joe Graedon,
pharmacologist & Teresa Graedon, nutrition expert
"Taking menopause
hormones for five years doubles the risk for
breast cancer,
according to a new analysis of a federal study that reveals the most dramatic
evidence yet of the dangers of these popular pills." - Marilynn Marchione
12/13/08
"Today's announcement that the
ENHANCE study failed to find
any positive benefit from the addition of
Zetia® to a common,
inexpensive, generic therapy raised concerns that attempts were made to mask
the minimal value of this new drug."- Representative John Dingell, Committee on
Energy and Commerce chairman 1/15/08
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